Evidence map›Paper›PMID 36567036›Full record

ArticleFertility and sterility2023

The developmental competence of human metaphase I oocytes with delayed maturation in vitro.

Jeong Hee Moon, Qianying Zhao, Jiaqi Zhang, Vik Reddy, Jinnou Han, Yuan Cheng, Nan Zhang, Jennifer Dasig, Liesl Nel-Themaat, Barry Behr and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Fertility and sterility, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Jeong Hee MoonStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Qianying ZhaoStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Jiaqi ZhangStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Vik ReddyStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Jinnou HanStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Yuan ChengStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Nan ZhangStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Jennifer DasigStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Liesl Nel-ThemaatStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California.
Barry BehrDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California.
Bo YuStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, California; Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California; Stanford Maternal and Child Health Research Institute, Stanford University School of Medicine, Stanford, California. Electronic address: byu1@stanford.edu.
Stanford Health Care · USStanford University · US

Funding

The role of fallopian tube microbiome in ovarian carcinogenesisK08CA222385 · NCI · UNIVERSITY OF WASHINGTON · PI YU, BO · 2018 to 2023
$1.1M
Genomic Instability and The Roles of P53 and P19arf in Pancreatic CancerK08CA122835 · NCI · UNIVERSITY OF ROCHESTER · PI HEZEL, ARAM F. · 2006 to 2010
$712k
Evaluation of ovarian reserve, aging and fertility preservation in women with sickle cell diseaseR21HD103034 · NICHD · STANFORD UNIVERSITY · PI YU, BO · 2020 to 2021
$434k
NCI NIH HHS K08 CA122835NCI NIH HHS K08 CA222385NICHD NIH HHS R21 HD103034
6 · The paper itself

Abstract

objectiveTo evaluate whether metaphase I (MI) oocytes completing maturation in vitro to metaphase II ("MI-MII oocytes") have similar developmental competence as the sibling metaphase II (MII) oocytes that reached maturity in vivo.

designRetrospective cohort study.

settingAcademic medical center. PATIENT(S): A total of 1,124 intracytoplasmic sperm injection (ICSI) cycles from 800 patients at a single academic center between April 2016 and December 2020 with at least 1 MII oocyte immediately after retrieval and at least 1 sibling "MI-MII oocyte" that was retrieved as MI and matured to MII in culture before ICSI were included in the study. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): A total of 7,865 MII and 2,369 sibling MI-MII oocytes retrieved from the same individuals were compared for the fertilization and blastocyst formation rates. For patients who underwent single euploid blastocyst transfers (n = 406), the clinical pregnancy, spontaneous pregnancy loss, and live birth rates were compared between the 2 groups. RESULT(S): The fertilization rate was significantly higher in MII oocytes than in delayed matured MI-MII oocytes (75.9% vs. 56.1%). Similarly, the blastocyst formation rate was higher in embryos derived from MII oocytes than in those from MI-MII oocytes (53.8% vs. 23.9%). The percentage of euploid embryos derived from MII oocytes was significantly higher than that of those from MI-MII oocytes (49.2% vs. 34.7%). Paired comparison of sibling oocytes within the same cycle showed higher developmental competence of the MII oocytes than that of MI-MII oocytes. However, the pregnancy, spontaneous pregnancy loss, and live birth rates after a single euploid blastocyst transfer showed no statistically significant difference between the 2 groups (MII vs. MI-MII group, 65.7% vs. 74.1%, 6.4% vs. 5.0%, and 61.5% vs. 70.0%, respectively). CONCLUSION(S): Compared with oocytes that matured in vivo and were retrieved as MII, the oocytes that were retrieved as MI and matured to MII in vitro before ICSI showed lower developmental competence, including lower fertilization, blastocyst formation, and euploidy rates. However, euploid blastocysts from either cohort resulted in similar live birth rates, indicating that the MI oocytes with delayed maturation can still be useful even though the overall developmental competence was lower than that of their in vivo matured counterparts.

Indexed as

Abortion, SpontaneousFemaleFertilization in VitroHumansMaleMetaphaseOocytesPregnancyRetrospective StudiesSemenfrozen embryo transfer (FET)metaphase II (MII)Metaphase I (MI)oocyte maturationsingle euploid blastocyst

Identifiers

PMID36567036
PMCPMC10436753
OpenAlexW4312193466

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.